BEUDAMED
    FDA Recall Terminated

    Stryker Medical Secure II Med/Surg Bed, 230 V, Stryker Medical, Portage, MI.; Model 3221 (not sold in the U.S.).

    Recall: Z-1688-2008 · Initiated February 1, 2008

    Recall

    Recall Number
    Z-1688-2008
    Event Number
    45908
    Firm
    Stryker Medical Div. of Stryker Corporation
    FEI Number
    1831750
    Product Code
    FNL
    Status
    Terminated
    Root Cause
    Device Design
    Initiated
    February 1, 2008
    Posted
    September 19, 2008
    Terminated
    November 5, 2010
    Address
    3800 E. Centre Ave., Portage, MI, 49002

    Description

    Stryker Medical Secure II Med/Surg Bed, 230 V, Stryker Medical, Portage, MI.; Model 3221 (not sold in the U.S.).

    Reason

    The brakes may not have adequate holding power to lock the bed in place.

    Action

    Consignees were notified via letter dated 2/1/08 and informed that upgrade kits along with full written and video installation instructions will be sent to correct the problem.

    Distribution

    Worldwide, Argentina, Brazil, Canada, Chile, China, Greece, India Japan, Mexico, Poland, Singapore, South Africa, South Korea, Switzerland, Taiwan and United Kingdom.

    Quantity

    66,558 of all models.